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Real-time evaluation of the independent analgesic efficacy of dexmedetomidine
BACKGROUND: Dexmedetomidine has analgesic properties, but the intraoperative analgesic effect of dexmedetomidine is often masked by the effects of other general anaesthetics. Therefore, the degree to which it reduces intraoperative pain intensity remains unclear. The objective of this double-blind,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985296/ https://www.ncbi.nlm.nih.gov/pubmed/36870944 http://dx.doi.org/10.1186/s12871-023-02022-2 |
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author | Wang, XiaoHua Zhang, SiYuan Wang, Chunxiu Huang, Yi Wu, Hao Zhao, Guoguang Wang, TianLong |
author_facet | Wang, XiaoHua Zhang, SiYuan Wang, Chunxiu Huang, Yi Wu, Hao Zhao, Guoguang Wang, TianLong |
author_sort | Wang, XiaoHua |
collection | PubMed |
description | BACKGROUND: Dexmedetomidine has analgesic properties, but the intraoperative analgesic effect of dexmedetomidine is often masked by the effects of other general anaesthetics. Therefore, the degree to which it reduces intraoperative pain intensity remains unclear. The objective of this double-blind, randomised controlled trial was to evaluate the independent intraoperative analgesic efficacy of dexmedetomidine in real-time. METHODS: This single-centre study enrolled 181 patients who were hospitalised for below-knee orthopaedic surgeries between 19 January 2021 to 3 August 2021 were eligible for this is single-centre study. Peripheral neural block was performed on patients scheduled for below-knee orthopaedic surgeries. Patients were randomly assigned to the dexmedetomidine or midazolam group and were intravenously administered with 1.5 µg kg(−1) h(−1) dexmedetomidine or 50 µg kg(−1) h(−1) midazolam, respectively. The analgesic efficacy was evaluated using the real-time non-invasive nociception monitoring. The primary endpoint was the attainment rate of the nociception index target. The secondary endpoints included the occurrence of intraoperative hypoxemia, haemodynamic parameters, the consciousness index, electromyography and patient outcomes. RESULTS: On Kaplan–Meier survival analysis, the defined nociception index target was attained in 95.45% and 40.91% of patients receiving dexmedetomidine and midazolam, respectively. Log-rank analysis revealed that the dexmedetomidine group attained the nociception index target significantly faster and the median attainment time of the nociception index target in the dexmedetomidine group was 15 min. Dexmedetomidine group was associated with a significantly lower incidence of hypoxemia. There was no significant difference in blood pressure between the dexmedetomidine and midazolam groups. Further, the dexmedetomidine group had a lower maximum visual analogue scale score and lower analgesic consumption postoperatively. CONCLUSIONS: Dexmedetomidine has independent analgesia and systemically administered as an adjuvant agent has better analgesic efficacy than midazolam without severe side effects. TRIAL REGISTRATION: clinicaltrial.gov Registry Identifier: NCT-04675372.Registered on 19/12 /2020. |
format | Online Article Text |
id | pubmed-9985296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99852962023-03-05 Real-time evaluation of the independent analgesic efficacy of dexmedetomidine Wang, XiaoHua Zhang, SiYuan Wang, Chunxiu Huang, Yi Wu, Hao Zhao, Guoguang Wang, TianLong BMC Anesthesiol Research BACKGROUND: Dexmedetomidine has analgesic properties, but the intraoperative analgesic effect of dexmedetomidine is often masked by the effects of other general anaesthetics. Therefore, the degree to which it reduces intraoperative pain intensity remains unclear. The objective of this double-blind, randomised controlled trial was to evaluate the independent intraoperative analgesic efficacy of dexmedetomidine in real-time. METHODS: This single-centre study enrolled 181 patients who were hospitalised for below-knee orthopaedic surgeries between 19 January 2021 to 3 August 2021 were eligible for this is single-centre study. Peripheral neural block was performed on patients scheduled for below-knee orthopaedic surgeries. Patients were randomly assigned to the dexmedetomidine or midazolam group and were intravenously administered with 1.5 µg kg(−1) h(−1) dexmedetomidine or 50 µg kg(−1) h(−1) midazolam, respectively. The analgesic efficacy was evaluated using the real-time non-invasive nociception monitoring. The primary endpoint was the attainment rate of the nociception index target. The secondary endpoints included the occurrence of intraoperative hypoxemia, haemodynamic parameters, the consciousness index, electromyography and patient outcomes. RESULTS: On Kaplan–Meier survival analysis, the defined nociception index target was attained in 95.45% and 40.91% of patients receiving dexmedetomidine and midazolam, respectively. Log-rank analysis revealed that the dexmedetomidine group attained the nociception index target significantly faster and the median attainment time of the nociception index target in the dexmedetomidine group was 15 min. Dexmedetomidine group was associated with a significantly lower incidence of hypoxemia. There was no significant difference in blood pressure between the dexmedetomidine and midazolam groups. Further, the dexmedetomidine group had a lower maximum visual analogue scale score and lower analgesic consumption postoperatively. CONCLUSIONS: Dexmedetomidine has independent analgesia and systemically administered as an adjuvant agent has better analgesic efficacy than midazolam without severe side effects. TRIAL REGISTRATION: clinicaltrial.gov Registry Identifier: NCT-04675372.Registered on 19/12 /2020. BioMed Central 2023-03-04 /pmc/articles/PMC9985296/ /pubmed/36870944 http://dx.doi.org/10.1186/s12871-023-02022-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, XiaoHua Zhang, SiYuan Wang, Chunxiu Huang, Yi Wu, Hao Zhao, Guoguang Wang, TianLong Real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
title | Real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
title_full | Real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
title_fullStr | Real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
title_full_unstemmed | Real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
title_short | Real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
title_sort | real-time evaluation of the independent analgesic efficacy of dexmedetomidine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985296/ https://www.ncbi.nlm.nih.gov/pubmed/36870944 http://dx.doi.org/10.1186/s12871-023-02022-2 |
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